Clamoxyl 200 mg ad us. vet.[E]

Hauptinformation

  • Handelsname:
  • Clamoxyl 200 mg ad us. vet.[E], Tabletten
  • Darreichungsform:
  • Tabletten
  • Verwenden für:
  • Tiere
  • Art der Medizin:
  • allopathic Droge

Dokumenten

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Clamoxyl 200 mg ad us. vet.[E], Tabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Tabletten für Hund und Katze gegen bakterielle Infektionen.

Weitere Informationen

Status

  • Quelle:
  • Institut für Veterinärpharmakologie
  • Zulassungsnummer:
  • 46389
  • Letzte Änderung:
  • 02-09-2017

Packungsbeilage

Clamoxyl 200 mg ad us. vet.

, Tabletten

Zoetis Schweiz GmbH

HINWEIS: Exportspezialität (Nur für den Vertrieb im Ausland zugelassen)!

Tabletten für Hund und Katze gegen bakterielle Infektionen.

ATCvet: QJ01CA04

Zusammensetzung

1 Tablette enthält:

Amoxicillinum anhydricum 200 mg

Excip. pro compr.

Fachinformationen Wirkstoffe (CliniPharm)

Amoxicillin

Eigenschaften / Wirkungen

Amoxicillin ist ein von Beecham aus dem Penicillinkern entwickeltes halbsynthetisches

Penicillin. Seine Eigenschaften sind:

Breites Wirkungsspektrum gegenüber einer Vielzahl von gramnegativen und

grampositiven Bakterien.

-Rasche bakterizide Wirkung.

Hervorragende Resorption nach peroraler Verabreichung und schnelle Bildung hoher

Serumtiter.

-Resorption wird durch Futteraufnahme kaum beeinträchtigt.

Rasche therapeutische Wirkung gegenüber einem breiten Spektrum bakterieller

Infektionen.

-Sehr schwache Toxizität.

-Hohe Konzentrationen in Galle und Urin.

Clamoxyl wirkt schnell bakterizid gegenüber einem breiten Spektrum von gramnegativen

und grampositiven bakteriellen Krankheitserregern, die bei Kleintieren auftreten:

Bordetella spp., Brucella spp., Clostridia spp., Corynebacterium spp., Escherichia coli,

Fusiformis spp., Haemophilus spp., Klebsiella spp., Moraxella spp., Pasteurella spp.,

Proteus mirabilis, Salmonella spp., Spirochaeten, einschliesslich Leptospira spp.,

Staphylokokken (Penicillinasebildner ausgenommen), Streptokokken und Vibrio spp.

Indikationen

Behandlung von Infektionen, die durch Amoxicillin-empfindliche Keime verursacht worden

sind, bei Hund und Katze:

Lokale Indikationen: Wunden, Hautinfektionen und Abszesse, bakterielle Dermatitiden,

Otitis.

Respiratorische Infektionen: Pneumonie, Bronchitis, Tonsillitis, Rhinitis, Laryngo-

Tracheitis.

Infektionen im Urogenitalbereich; Puerperalinfektionen: Metritis; Nephritis; Zystitis und

Vaginitis.

-Infektionen des Verdauungstraktes: Cholangiohepatitis, Gastro-Enteritis.

-Sekundäre bakterielle Infektionen z.B. nach Staupe.

-Allgemeininfektionen: Gelenks- und Nabelinfektionen.

-Antibiotischer Schutz bei chirurgischen Eingriffen.

Nachbehandlung nach parenteraler Behandlung mit Clamoxyl in schweren Fällen, z.B.

bei Septikaemien.

Wichtig: Bei akuten Infektionen soll die Behandlung mit Clamoxyl

-Injektionen eingeleitet

werden.

Dosierung: Hund, Katze: 4 - 10 mg pro kg KGW zweimal täglich während zwei bis fünf

Tagen peroral verabreichen. Bei schweren oder akuten Erkrankungen kann die Dosis

erhöht und/oder in kürzeren Intervallen wiederholt werden. Für die Behandlung von

gramnegativen Infektionen und bei Jungtieren wird im allgemeinen die höhere Dosierung

empfohlen.

KGW Amoxicillin-Dosis Clamoxyl 40 mg

Clamoxyl 200 mg

(kg)

(mg)

(Anzahl Tbl. pro Beh.)(Anzahl Tbl. pro Beh.)

5 kg 20 - 50 mg

⁄ - 1 Tbl.

10 kg40 - 100 mg

1 - 2 ⁄ Tbl.

⁄ - ⁄ Tbl.

20 kg80 - 200 mg

2 - 5 Tbl.

⁄ - 1 Tbl.

30 kg120 - 300 mg

⁄ - 1 ⁄ Tbl.

40 kg160 - 400 mg

1 - 2 Tbl.

50 kg200 - 500 mg

1 - 2 ⁄ Tbl.

Verabreichung: Die Kautabletten werden ganz eingegeben. Bei schwer erkrankten Tieren

können sie zerdrückt und mit Flüssigkeit verabreicht werden.

Normalerweise tritt innerhalb von drei Tagen nach Beginn der Behandlung eine Besserung

ein. Sollte in diesem Zeitraum ein Therapieerfolg ausbleiben, ist die Diagnose zu

überprüfen und die Therapie eventuell zu ändern.

Anwendungseinschränkungen

Kontraindikationen:

Clamoxyl soll nicht an penicillinempfindliche Tiere verabreicht werden.

Clamoxyl Tabletten nicht bei Kaninchen, Chinchilla, Meerschweinchen, Hamster und

anderen sehr kleinen Pflanzenfressern einsetzen.

Nicht bei Tieren anwenden, die der Gewinnung von Lebensmitteln dienen.

Unerwünschte Wirkungen

VetVigilance: Pharmacovigilance-Meldung erstatten

Die Anwendung von Beta-Laktamantibiotika kann allergische Reaktionen auslösen.

Sonstige Hinweise

Das Präparat darf nur bis zu dem auf der Packung mit "Exp" bezeichneten Datum

verwendet werden.

Bei Raumtemperatur (15 - 25°C) und vor Feuchtigkeit geschützt lagern.

Ausserhalb der Reichweite von Kindern aufbewahren.

Packungen

Nur für den Vertrieb im Ausland bestimmt.

Exportspezialität: Vertrieb in der Schweiz nicht zugelassen!

Abgabekategorie: A

Swissmedic Nr. 46'389

Informationsstand: 06/2005

Dieser Text ist behördlich genehmigt.

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21-9-2018

Umsetzung des einstimmigen Beschlusses der Koordinierungsgruppe EMA/CMDh/407069/2018 vom 27.06.2018 betreffend die Zulassungen für Humanarzneimittel mit dem Wirkstoff Deoxycholsäure

Umsetzung des einstimmigen Beschlusses der Koordinierungsgruppe EMA/CMDh/407069/2018 vom 27.06.2018 betreffend die Zulassungen für Humanarzneimittel mit dem Wirkstoff Deoxycholsäure

Das BfArM veröffentlicht den Umsetzungsbescheid für den Wirkstoff Deoxycholsäure infolge des Europäischen PSUR Single Assessment Verfahrens nach Artikel 107d) bis g) der Richtlinie 2001/83/EG.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

20-9-2018

Getinge Issues Worldwide Voluntary Correction of Maquet/Getinge Cardiosave Intra-Aortic Balloon Pump (IABP) For Interruption and/or Inability to Start Therapy at Altitudes above 3,200 Feet/975 Meters

Getinge Issues Worldwide Voluntary Correction of Maquet/Getinge Cardiosave Intra-Aortic Balloon Pump (IABP) For Interruption and/or Inability to Start Therapy at Altitudes above 3,200 Feet/975 Meters

Getinge is voluntarily initiating a Worldwide recall involving a field correction of approximately 5,223 Maquet/Getinge Cardiosave Intra-Aortic Balloon Pumps (IABP) sold by Datascope Corp., for a potential interruption and/or inability to start therapy to the patient regarding the use of certain Intra-Aortic Balloons (IABs) prior to or during the use with Cardiosave IABP for users who are at altitudes above 3200 feet/975 meters. This condition could potentially lead to patient hemodynamic instability.

FDA - U.S. Food and Drug Administration

20-9-2018

Drontal Plus Tasty ad us. vet., Tabletten fuer Hunde

Drontal Plus Tasty ad us. vet., Tabletten fuer Hunde

● Die Neuzulassung erfolgte am 20.09.2018.

Institut für Veterinärpharmakologie und toxikologie

20-9-2018

Euthoxin 500 mg/ml ad us. vet., Injektionsloesung

Euthoxin 500 mg/ml ad us. vet., Injektionsloesung

● Die Neuzulassung erfolgte am 20.09.2018.

Institut für Veterinärpharmakologie und toxikologie

19-9-2018

Danish Medicines Agency aces European benchmark survey

Danish Medicines Agency aces European benchmark survey

The Danish Medicines Agency has just scored 4.5 of a possible 5 in the common-European survey known as the Benchmarking of European Medicines Agencies (BEMA). ”It's a really good result that will benefit all of us and may help raise the standard throughout Europe,” said the Danish health minister.

Danish Medicines Agency

19-9-2018

Modification of the existing maximum residue levels for potassium phosphonates in certain berries and small fruits

Modification of the existing maximum residue levels for potassium phosphonates in certain berries and small fruits

Published on: Tue, 18 Sep 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant LTZ Augustenberg submitted a request to the competent national authority in Germany to modify the existing maximum residue levels (MRLs) for the active substance potassium phosphonates in raspberries, blackberries, currants, blueberries, gooseberries and elderberries. The data submitted in support of the request were found to be sufficient to derive MRL proposals for all crops under c...

Europe - EFSA - European Food Safety Authority Publications

19-9-2018

Modification of the existing maximum residue levels for flonicamid in various root crops

Modification of the existing maximum residue levels for flonicamid in various root crops

Published on: Tue, 18 Sep 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the Agriculture and Horticulture Development Council submitted a request to the competent national authority in the United Kingdom to modify the existing maximum residue levels (MRL) for the active substance flonicamid in beetroots, carrots, celeriacs/turnip rooted celeries, horseradishes, Jerusalem artichokes, parsnips, parsley roots/Hamburg roots parsley, radishes, salsifies, swedes/rutabagas, tu...

Europe - EFSA - European Food Safety Authority Publications

19-9-2018

National dietary survey in 2012‐2016 on the general population aged 1‐79 years in the Netherlands

National dietary survey in 2012‐2016 on the general population aged 1‐79 years in the Netherlands

Published on: Tue, 18 Sep 2018 00:00:00 +0200 During the years 2012‐2016, the Dutch National Food Consumption survey was conducted in the Netherlands. For the survey, a random sample was drawn from consumer panels stratified by age and gender and maintained representative to the population with regard to region, address density and educational level. Complete results were obtained for 4,313 persons (response rate 65%); including toddlers, children, adolescents, adults and elderly. Pregnant or lactating ...

Europe - EFSA - European Food Safety Authority Publications

19-9-2018

Umsetzung der einstimmigen Beschlüsse der Koordinierungsgruppe EMA/CMDh/33058/2017 vom 25.01.2017 und EMA/CMDh/413850/2018 vom 27.06.2018 betreffend die Zulassungen für Humanarzneimittel mit dem Wirkstoff Treprostinil

Umsetzung der einstimmigen Beschlüsse der Koordinierungsgruppe EMA/CMDh/33058/2017 vom 25.01.2017 und EMA/CMDh/413850/2018 vom 27.06.2018 betreffend die Zulassungen für Humanarzneimittel mit dem Wirkstoff Treprostinil

Das BfArM veröffentlicht den Umsetzungsbescheid für den Wirkstoff Treprostinil infolge des Europäischen PSUR Single Assessment Verfahrens nach Artikel 107d) bis g) der Richtlinie 2001/83/EG.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

19-9-2018

Umsetzung des einstimmigen Beschlusses der Koordinierungsgruppe EMA/CMDh/154226/2018 vom 21.03.2018 betreffend die Zulassungen für Humanarzneimittel mit dem Wirkstoff Oxytocin

Umsetzung des einstimmigen Beschlusses der Koordinierungsgruppe EMA/CMDh/154226/2018 vom 21.03.2018 betreffend die Zulassungen für Humanarzneimittel mit dem Wirkstoff Oxytocin

Das BfArM veröffentlicht den Umsetzungsbescheid für den Wirkstoff Oxytocin infolge des Europäischen PSUR Single Assessment Verfahrens nach Artikel 107d) bis g) der Richtlinie 2001/83/EG.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

18-9-2018

Lidl Voluntarily Recalls Bellona Brand Hazelnut Wafers Due to Improperly Declared Wheat Allergen

Lidl Voluntarily Recalls Bellona Brand Hazelnut Wafers Due to Improperly Declared Wheat Allergen

Lidl US has voluntarily recalled all Bellona brand “Milk Chocolate Flavored Coated Wafer with Hazelnut Crème Filling and White Chocolate Flavor” confections as a precautionary measure because the allergen statement does not include wheat.

FDA - U.S. Food and Drug Administration

18-9-2018

Xtava recalls Allure and Allure Pro 2200W ionic ceramic hair dryers

Xtava recalls Allure and Allure Pro 2200W ionic ceramic hair dryers

The hair dryer and power cord can overheat and catch on fire, posing fire, burn and electrical shock hazards.

Health Canada

18-9-2018

Peer review of the pesticide risk assessment of the active substance sodium hydrogen carbonate

Peer review of the pesticide risk assessment of the active substance sodium hydrogen carbonate

Published on: Fri, 14 Sep 2018 00:00:00 +0200 The conclusions of EFSA following the peer review of the initial risk assessments carried out by the competent authority of the rapporteur Member State Austria for the pesticide active substance sodium hydrogen carbonate are reported. The context of the peer review was that required by Regulation (EC) No 1107/2009 of the European Parliament and of the Council. The conclusions were reached on the basis of the evaluation of the representative use of sodium hyd...

Europe - EFSA - European Food Safety Authority Publications

19-10-2018

New Safety Communication. @US_FDA   is sharing Updated Information To Reduce Potential Cardiac Surgery   Infection Risks Associated With the LivaNova 3T Heater-Cooler Systems. Read More:  https://go.usa.gov/xPnNW  #FDA #MedicalDevice

New Safety Communication. @US_FDA is sharing Updated Information To Reduce Potential Cardiac Surgery Infection Risks Associated With the LivaNova 3T Heater-Cooler Systems. Read More: https://go.usa.gov/xPnNW  #FDA #MedicalDevice

New Safety Communication. @US_FDA is sharing Updated Information To Reduce Potential Cardiac Surgery Infection Risks Associated With the LivaNova 3T Heater-Cooler Systems. Read More: https://go.usa.gov/xPnNW  #FDA #MedicalDevice

FDA - U.S. Food and Drug Administration

17-10-2018

Save the date & Join the @US_FDA’s  Patient Engagement Advisory Committee on Nov 15th to discuss  patient-generated health data from sources like social media, activity  trackers, and patient-driven registries. Learn more:  https://go.usa.gov/xPRau  #Digi

Save the date & Join the @US_FDA’s Patient Engagement Advisory Committee on Nov 15th to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries. Learn more: https://go.usa.gov/xPRau  #Digi

Save the date & Join the @US_FDA’s Patient Engagement Advisory Committee on Nov 15th to discuss patient-generated health data from sources like social media, activity trackers, and patient-driven registries. Learn more: https://go.usa.gov/xPRau  #DigitalHealth #PEAC2018 pic.twitter.com/NU61Snpxxw

FDA - U.S. Food and Drug Administration

15-10-2018

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4.

 http://fema.gov/hurricane-michael-rumor-co

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4. http://fema.gov/hurricane-michael-rumor-co

We have created a rumor control page for Hurricane #Michael that will be updated regularly. Help us share this info and remember to always check with official sources like @FLSERT, @GeorgiaEMA and @femaregion4. http://fema.gov/hurricane-michael-rumor-control … pic.twitter.com/T3h7ZiFUrZ

FDA - U.S. Food and Drug Administration

10-10-2018

Diversity in research means more treatments work for more people. Join #ResearchDiversity Day on October 23rd for a day-long discussion of diversity in study recruitment and research. Join us! @Alzheimers_NIHpic.twitter.com/AwYhetCBiw

Diversity in research means more treatments work for more people. Join #ResearchDiversity Day on October 23rd for a day-long discussion of diversity in study recruitment and research. Join us! @Alzheimers_NIHpic.twitter.com/AwYhetCBiw

Diversity in research means more treatments work for more people. Join #ResearchDiversity Day on October 23rd for a day-long discussion of diversity in study recruitment and research. Join us! @Alzheimers_NIH pic.twitter.com/AwYhetCBiw

FDA - U.S. Food and Drug Administration

17-9-2018

Scientific guideline:  Concept paper on the need for revision of the guideline on the investigation of medicinal products in the term and preterm neonate - Revision 1, draft: consultation open

Scientific guideline: Concept paper on the need for revision of the guideline on the investigation of medicinal products in the term and preterm neonate - Revision 1, draft: consultation open

The Guideline on the investigation of medicinal products in the term and preterm neonates was prepared during the period from 2007 to 2009 and came into effect in 2010 (EMEA/536810/2008). Considerable experience of assessing PIP applications covering neonatal age subset has been gained since then and it has become apparent that some essential questions arise repeatedly during the assessment of Paediatric Investigation Plans (PIP) applications for products intended to be investigated and used in neonates....

Europe - EMA - European Medicines Agency